Banana fruit VQ motif-containing protein5 represses cold-responsive transcription factor MaWRKY26 involved in the regulation of JA biosynthetic genes

• Published in: Scientific reports 2016-03, Vol.6 (1), p.23632-23632, Article 23632
• Main Authors: Ye, Yu-Jie, Xiao, Yun-Yi, Han, Yan-Chao, Shan, Wei, Fan, Zhong-Qi, Xu, Qun-Gang, Kuang, Jian-Fei, Lu, Wang-Jin, Lakshmanan, Prakash, Chen, Jian-Ye
• Format: Article
• Language: English
• Subjects: 38/39; 38/77; 631/449/1741/2671; 631/449/2661/2665; 82/29; 82/80; 96/35; Biosynthesis; Biosynthetic Pathways; Cell Nucleus - metabolism; Chilling; Cold Temperature; Cold tolerance; Cyclopentanes - metabolism; Fruits; Gene Expression Regulation, Plant; Gene regulation; Humanities and Social Sciences; Jasmonic acid; Low temperature; Methyl jasmonate; multidisciplinary; Musa - metabolism; Musa - physiology; Oxylipins - metabolism; Plant hormones; Plant Proteins - genetics; Plant Proteins - metabolism; Promoter Regions, Genetic; Promoters; Protein Binding; Science; Stress, Physiological; Temperature effects; Transcription activation; Transcription factors; Transcription Factors - genetics; Transcription Factors - metabolism; Vegetables
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep23632

Most harvested fruits and vegetables are stored at low temperature but many of them are highly sensitive to chilling injury. Jasmonic acid (JA), a plant hormone associated with various stress responses, is known to reduce chilling injury in fruits. However, little is known about the transcriptional regulation of JA biosynthesis in relation to cold response of fruits. Here, we show the involvement of a Group I WRKY transcription factor (TF) from banana fruit, MaWRKY26, in regulating JA biosynthesis. MaWRKY26 was found to be nuclear-localized with transcriptional activation property. MaWRKY26 was induced by cold stress or by methyl jasmonate (MeJA), which enhances cold tolerance in banana fruit. More importantly, MaWRKY26 transactivated JA biosynthetic genes MaLOX2, MaAOS3 and MaOPR3 via binding to their promoters. Further, MaWRKY26 physically interacted with a VQ motif-containing protein MaVQ5 and the interaction attenuated MaWRKY26-induced transactivation of JA biosynthetic genes. These results strongly suggest that MaVQ5 might act as a repressor of MaWRKY26 in activating JA biosynthesis. Taken together, our findings provide new insights into the transcriptional regulation of JA biosynthesis in response to cold stress and a better understanding of the molecular aspects of chilling injury in banana fruit.